The case
Sara is a 41-year-old secretary in an autobody shop who comes to see you for evaluation of intermittent episodes of wheezing and shortness of breath that have progressed over the past 2 years. She feels that she has more “colds” than her workplace colleague. Each episode lasts for 2–3 weeks, with persistent cough and dyspnea. She had wheezing and allergy symptoms in childhood, and her mother and 1 cousin have confirmed asthma. Over the past 6 months, she has noticed that because of her dyspnea, she is unable to keep up with her partner when they go salsa dancing. She is otherwise well and is taking no medications. She smokes a half package of cigarettes daily and has done so for 20 years.
When you first saw Sara a few weeks ago, you gave her a salbutamol inhaler; in addition, you arranged spirometry, both before and after administration of a bronchodilator. She reports that she has been using the salbutamol daily for dyspnea and when she wakens during the night with similar symptoms; the latter is still a weekly occurrence. Spirometry shows a mild obstructive defect, with forced expiratory volume in 1 second (FEV1) of 2.29 L (78% of predicted), forced vital capacity of 3.48 L (99% of predicted), a FEV1/FVC ratio of 66% and a 17% improvement in FEV1 after administration of an inhaled bronchodilator. You make a diagnosis of asthma. What is your proposed management?
Asthma remains the most common chronic disease of young adults, and the age-adjusted prevalence of this condition in Canada and other industrialized countries has continued to rise over the past 2 decades. 1 Despite the increase in prevalence, asthma-related mortality in Canada has fallen steadily over the past 20 years; 2 nonetheless, poor control of asthma symptoms continues to contribute to unnecessary morbidity, including unscheduled physician visits, days missed from work or school, limitation of daily activities and impairment of quality of life. 3 Canadian guidelines for the diagnosis and treatment of asthma have existed since 1989 and were most recently updated in 2003. 4 In this series, we are using case-based examples to highlight recent changes in recommendations for asthma management and to highlight practical aspects of diagnosis and treatment. The case used here focuses on the management of asthma in adults.
In this article, we discuss the following major changes in the management of asthma (since the 2003 update): the use of budesonide and formoterol in a single inhaler for both maintenance and reliever therapy; the earlier introduction of inhaled corticosteroid therapy in the treatment of mild asthma; the possible role of intermittent inhaled corticosteroid therapy for mild asthma; the importance of exploring the possibility of work-related asthma; and the role of obesity in asthma.
In addition, we re-emphasize the following important points about the diagnosis and treatment of asthma, as set out in previous guidelines: the importance of controlling contributing factors (e.g., environment, gastroesophageal reflux, sinus disease) in terms of achieving control, the primary role of inhaled corticosteroid monotherapy in the initial maintenance therapy of asthma, the importance of regular follow-up for asthma and attention to parameters of asthma control, and contraindications to regular monotherapy with long-acting β2-agonists.
We employed a comprehensive approach, involving several search strategies, as described in detail in a previous article in this series, 5 to identify studies published since the appearance of the 2003 Canadian asthma guidelines. 4 We based our grades of evidence on those of the Canadian Task Force on Preventive Health Care, 6 as described previously. 5
Initial management of untreated asthma
Six main principles of asthma management are common for all patients: 7 environmental control, regular anti-inflammatory therapy, appropriate use of inhalation therapy, consultation with a certified asthma educator, graduated approach to therapy (including “reliever” medication) and regular follow-up with the physician. These principles are illustrated in the asthma continuum (Figure 1) and explained in more detail below.
Environmental control and asthma education are critical but often neglected components of management. A thorough clinical history should be obtained, including details about the patient’s home and work environments, with particular attention to known allergens, including pets, moulds and house dust mites (Table 1). Allergy testing should be considered. Smoking cessation and avoidance of second-hand smoke are also important.
Health care providers understand asthma as a chronic inflammatory disease provoking variable airflow obstruction and symptoms. Patients, however, often do not appropriately understand why the chronic nature of asthma makes adherence to maintenance anti-inflammatory therapy essential. The patient should be educated about the need for regular anti-inflammatory therapy, rather than sporadic relief of symptoms with bronchodilators.
Inhalation therapy is the cornerstone of asthma management, but many patients do not readily master the proper use of inhalers. All health care professionals should learn appropriate inhaler technique so that they can demonstrate these techniques to their patients and observe how patients perform them at all visits. Representative videos illustrating appropriate inhaler technique can be found at www.on.lung.ca/Health-Care-Professionals/Provider-Education-Program/CD-ROMS.php.
Whenever possible, people with asthma should be referred to a certified asthma educator, a health care professional who has completed specialized training and passed a certification examination that covers methods of teaching asthma management, as well as aspects of learning and behavioural techniques. Such a service complements visits to the physician and ensures that patients receive consistent education about their disease. During these sessions, the educator reviews the patient’s knowledge about asthma and provides a written action plan outlining how and when to adjust treatment. The educator prepares the plan, which is based on control or worsening of the patient’s asthma, in consultation with the primary care physician. If a certified asthma educator is not available, the physician who is managing the patient’s asthma should prepare the written action plan.
The continuum of asthma management (Figure 1) outlines a graduated approach to therapy and illustrates the need for “reliever” medication (i.e., a rapid-acting β2-agonist) for immediate relief of symptoms and “controller” medication (i.e., anti-inflammatory) for ongoing disease management. Every person with a diagnosis of asthma should be given a rapid-acting β2-agonist for as-needed relief, and the large majority should be given an anti-inflammatory controller medication for regular use.
Long-term compliance with controller therapy is poor, because patients tend to stop therapy when their symptoms subside. Therefore, regular follow-up visits are important. At these visits, the physician should reassess asthma control, as well as any barriers to control, including lack of adherence with anti-inflammatory medication. Control should be assessed frequently, and the maintenance dose adjusted to the minimum required to maintain control. At each visit, compliance, inhaler technique, triggers, environment and comorbidities should be assessed.
Environmental interventions
Environmental exposures trigger symptoms and exacerbations of asthma. Previous asthma guidelines have recommended skin testing to common aeroallergens to help identify which allergen may be most relevant for a specific patient. 4,8 Testing should be performed for the common indoor and outdoor aeroallergens that are pertinent to the patient’s geographic region. These allergens may include house dust mite, cat, dog, cockroach, moulds and pollens. Reducing exposure to an allergen to which the patient is sensitized may improve asthma control and reduce the need for medication. 8 However, allergen-avoidance measures may be labour-intensive, making adherence difficult and necessitating frequent reassessment and encouragement by treating physicians. Suggested questions for an indoor environmental history are listed in Table 1.
Most studies examining single-strategy interventions aimed at reducing exposure to single allergens have demonstrated no measurable benefits in asthma control. 9 However, the concurrent use of several interventions individually tailored to known allergens has yielded significant benefit for children. 10 Examples of such tailored interventions include use of allergen-impermeable covers for furniture and bedding, use of a vacuum cleaner equipped with a high-efficiency particulate air filter, use of a high-efficiency particulate air purifier in a child’s bedroom if the child is exposed to second-hand smoke or is sensitized and exposed to cat or dog allergens or mould, and professional pest control for the homes of children sensitized and exposed to cockroach allergen. Although large randomized trials assessing interventions for multiple allergens in adults have not been performed, avoidance of identified allergens is usually recommended for adults with allergic asthma.
House dust mites are ubiquitous in humid environments. They are difficult to control and impossible to eliminate. Efforts to reduce mite allergens — including encasing mattresses, replacing carpet with hard-surface flooring, removing as many dust-gathering objects as possible and using high-efficiency particulate air filtration systems or chemicals — have been disappointing 11 and should not be broadly recommended in isolation.
Although randomized controlled trials of avoidance of animal allergens have not been conducted, pets should be eliminated from the homes of people who have asthma and confirmed animal allergies. However, compliance with this recommendation is poor, and it may take many months for the allergen load to decline after an animal has been removed. 12
Cockroach allergens are known triggers of asthma, 13 and elimination may be valuable from the perspectives of both asthma control and general hygiene.
Moulds constitute a source of airborne allergens associated with worsening of asthma. Cleaning with fungicides, de-humidification to less than 50% humidity, high-efficiency particulate air filtration and central air conditioning may reduce the antigen load and severe symptoms of asthma in individuals with known fungal allergies. 14
Smoking and exposure to smoke
Active smoking by patients with asthma is associated with worsening of symptoms and accelerated decline in lung function. 15 Cigarette smoking may modify the inflammatory response in asthma and may be responsible for the decrease in response to inhaled corticosteroids that is typically observed among smokers. 15 Exposure to environmental or second-hand smoke is associated with adverse outcomes in both children and adults with asthma. 8,16
Reliever medications
Inhaled rapid-acting β2-agonists act on the β-adrenergic receptors in the airways, leading to relaxation of the smooth muscles of the airway. These medications should be used to treat acute bronchoconstriction during exacerbations of asthma. 7 They may also be used before exercise to prevent symptoms of exertion-induced bronchoconstriction. 17 Salbutamol and terbutaline have been available as reliever medications for many years. The long-acting β2-agonist formoterol is unique in that it also has a rapid onset of action and can therefore be used to relieve acute symptoms. However, regular use of long-acting β2-agonists as monotherapy has been associated with increased morbidity and mortality and should be avoided. 18–20
Initial controller medications
Inhaled corticosteroids
Inhaled corticosteroids (Table 2) 8 are the most effective maintenance treatment for asthma and represent the standard of care. 7 Regular use of inhaled corticosteroids decreases symptoms and exacerbations and improves the results of spirometry and the patient’s quality of life. 8
Low-dose inhaled corticosteroid monotherapy is recommended as first-line maintenance therapy for most patients with asthma. 4,7 The addition of long-acting β2-agonists has not improved clinical outcomes for patients whose asthma is well controlled with low-dose inhaled corticosteroids, 21,22 and, for most patients with asthma, there is no indication for using combination therapy as initial maintenance therapy.
Low- or moderate-dose inhaled corticosteroid therapy is generally free of serious adverse effects but may cause local or systemic adverse effects. Local adverse effects include oral thrush and dysphonia. The incidence of oral thrush with the use of inhaled corticosteroids depends on the particular drug, the dose and the delivery system. Rates in controlled trials ranged from 0% to 5% and appeared highest with fluticasone, 23 but the methods used (visual scores alone v. culture) have varied substantially among trials, which makes it difficult to compare medications. The risk of oral candidiasis may be greatly reduced by rinsing and spitting after inhaling the medication or by using a valved holding chamber. The incidence of dysphonia has ranged from 2% to 6% in clinical trials. This adverse effect is dose-dependent and may be related to reversible myopathy of the vocal cords. Both of these local adverse effects may occur less frequently with the pro-drug ciclesonide because most of the conversion to the active compound, desisobutyryl-ciclesonide, occurs in the lung. 24 Systemic adverse effects are uncommon and include adrenal suppression, changes in bone density, cataracts, glaucoma and growth retardation. 25,26 Because of the very low systemic exposure to steroids, these adverse events are rare, occurring in less than 1% of users. Bruising is slightly more common, particularly in older patients and those using higher doses. Valved holding chambers may reduce systemic adverse effects as well, but not those caused by absorption of the drugs after delivery to the lungs.
Leukotriene receptor antagonists
The leukotriene receptor antagonists are a class of non-steroidal anti-inflammatory asthma medications that are safe and well tolerated. Drugs from this class that are available in Canada include montelukast and zafirlukast. These medications act by specifically blocking the cysteinyl leukotriene receptor-1 receptors. When taken regularly they can be effective in the treatment of asthma. 27 However, they are less effective than inhaled corticosteroids; therefore, if they are used as monotherapy, they should be reserved for patients who cannot or will not take inhaled corticosteroids and for those in whom inhaled corticosteroids have had no benefit. 4,28
The case continued
The course of treatment for Sara is now clear, given the diagnosis and the available treatment options. You should take the following steps:
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Discuss smoking cessation with Sara and offer referral to a smoking cessation clinic. Consider prescribing smoking cessation aids, such as nicotine replacement, bupropion or varenicline.
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Counsel Sara about her disease, or refer her to a certified asthma educator at a local asthma centre, if available.
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Offer Sara both verbal and written asthma education, including a written action plan (for an example, see Appendix 1, at www.cmaj.ca/cgi/content/full/cmaj.080007/DC1); this may be performed by the asthma educator, if available.
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Prescribe a low dose of an inhaled corticosteroid (budesonide 200 μg one inhalation twice daily or ciclesonide 200 μg one inhalation every morning or fluticasone 125 μg one inhalation twice daily), along with a rapid-acting β2-agonist for use as a rescue medication.
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Arrange a follow-up visit with Sara in 4 to 6 weeks to assess her asthma control (Box 1), to review her inhaler technique and to determine the clinical response.
When Sara returns 6 weeks later, she tells you that she “feels fine.” However, she reports that salsa dancing still leaves her winded and precipitates coughing. About once a week, she wakes up at 3 am feeling short of breath but feels better after taking a puff of salbutamol.
Is Sara’s asthma under acceptable control?
The most important part of any follow-up visit with a patient who has asthma is to review control of the disease by specifically asking the questions listed in Box 1 as a list. According to these criteria, the fact that Sara is still experien cing exercise limitations and weekly nocturnal awakenings (i.e., missing 2 criteria) indicates that her asthma remains uncontrolled. Uncontrolled asthma is associated with a greater frequency of adverse outcomes than is well-controlled asthma, including exacerbations requiring visits to the emergency department and admission to hospital. 29
Treating uncontrolled asthma
For a patient whose asthma is inadequately controlled, the physician must use a series of specific questions to determine the cause:
1. Is the diagnosis correct?
Confirm the diagnosis with spirometry testing before and after administration of a bronchodilator if this has not previously been done. In Sara’s case, this testing was done at the time of her diagnosis.
2. Is the patient taking his or her medications?
Nonadherence to prescribed inhaled medications is common among patients with asthma, as it is for patients with many chronic lung diseases. Sara says that she has missed only the occasional dose of inhaled corticosteroid and shows you her inhaler device. You see that she has already refilled the initial prescription, given 6 weeks ago. This suggests that she is using the medication.
3. Is the patient’s inhaler technique adequate?
Sara saw an asthma educator when asthma was originally diagnosed. At that time, the educator explained the pathogenesis of the disease and the need for long-term anti-inflammatory therapy. In addition, the asthma educator reviewed proper inhaler technique and chose an appropriate delivery device for Sara. A review of her technique in the office reveals that she is using her current device well.
4. Is the patient exposed to allergens, irritants or occupational sensitizers?
Sara confirms that she has not smoked since her last visit to you but admits that she is anxious and still craves cigarettes. Cigarette smoking leads to poor asthma control and an accelerated loss of lung function, and impairs the effectiveness of inhaled corticosteroid therapy. 15 Smoking cessation is essential if good control of asthma is to be achieved.
Work-related asthma is frequent among adults with asthma. 30 Work-related asthma encompasses occupational asthma, which is caused by a specific work exposure (caused by sensitization, an immunologic response or exposure to a high-level irritant at work), and work-exacerbated asthma, which has non-work-related causes but is worsened by exposures at work. Common work settings associated with occupational asthma include health care, work with diisocyanates (e.g., production of polyurethane foam or use of spray paints) and work with animals, food or wood. Both occupational asthma and work-exacerbated asthma should be carefully investigated, starting with a detailed history (Box 2), 31 although the historical features listed in Box 2 are not specific for occupational asthma. 32
Detailed investigations usually require referral to a specialist and should be initiated early, while the patient is still working. A diagnosis of work-related asthma may have substantial occupational and psychosocial implications, and the patient should not be advised to leave work until a diagnosis has been confirmed as far as possible by a specialist. If the patient has work-related asthma, some modifications may be required to reduce exposure at work, and a change in work-place may occasionally be required.
Sara has told you that she works in an autobody shop, a setting where sprays containing diisocyanate are frequently used, but her work is in a well-ventilated area where she is not exposed to dust or fumes. She has not noticed her symptoms worsening during the course of the work week.
5. Does the patient have ongoing nasal symptoms?
The upper and lower airways form a continuum, such that anything that inflames the upper airways will worsen control of asthma. Sara has noted nasal stuffiness in the past, which she attributed to renovations in her apartment complex a few years ago, but she denies any sinus pain or a sensation of postnasal drip or nasal stuffiness at the present time.
6. Does the patient have gastresophageal reflux disease?
The association between gastresophageal reflux disease and asthma is well established, 33 although the evidence that treating reflux improves asthma control is still equivocal. 34 Treating reflux seems to improve certain symptoms of asthma, particularly a cough that is bothersome for the patient, but it does not usually lead to an improvement in the results of spirometry.
7. Is the patient taking a medicine that could worsen asthma?
About 10% of people with asthma will experience worsening of symptoms with nonsteroidal anti-inflammatory drugs. 35 There may also be some worsening with β-blockers, although this is less likely with the newer β1-specific agents (e.g., atenolol, bisoprolol, metoprolol). 36
8. Is the patient obese?
Obesity is associated with an increased risk of asthma, particularly among women. 37 Preliminary evidence suggests that weight loss improves some outcomes of asthma. 38 Sara has a body mass index of 23, so no further discussion of diet or weight loss is entertained.
9. Does the patient have a serious complication of asthma?
Severe consequences of asthma such as allergic bronchopulmonary aspergillosis and Churg–Strauss vasculitis are rare; they will be discussed in a subsequent article in this series.
Now that you have considered and addressed all other causes of poor asthma control in this case, you decide to augment Sara’s therapy.
Optimizing therapy
Is it better to increase the dose of inhaled corticosteroids or to add another class of medication?
Inhaled corticosteroids have a relatively flat dose–response curve. Although some patients benefit from higher doses of inhaled corticosteroids, there are no readily available clinical tools to identify such patients in advance. Therefore, if asthma is not controlled (Box 1) in a patient who is adherent with therapy (dose equivalent to fluticasone 250 μg/day), it is recommended to add another class of medication, usually a long-acting β2-agonist, rather than increasing the dose of inhaled corticosteroid. It is important to reiterate that adherence to inhaled corticosteroids is often poor; therefore, before prescribing an additional drug, the treating clinician must reassess adherence to the prescribed dosage of inhaled corticosteroid and, if necessary, counsel the patient regarding barriers to and improvement of adherence.
Which is the best therapy to add to inhaled corticosteroids?
Adding a long-acting β2-agonist to low-dose inhaled corticosteroids leads to fewer exacerbations, a decreased need for reliever medication, fewer nocturnal symptoms and improved quality of life, relative to doubling the dose of inhaled corticosteroid. 19,39 Similarly, adding a leukotriene receptor antagonist to inhaled corticosteroids yields better results than the use of either agent alone. 40,41 The main question is which medication to add. Most studies favour the combination of inhaled corticosteroid and long-acting β2-agonist because of greater improvements in lung function 42 and a higher response rate than occurs with the addition of leukotriene or a further increase in the dose of inhaled corticosteroid. Also, these 2 drugs can be combined in the same delivery device, which may improve adherence and decrease the likelihood that the patient will stop using the inhaled corticosteroid, thereby guarding against the potential risks of long-acting β2-agonist monotherapy. Inhaled corticosteroids remain the most important component of asthma controller therapy.
Some patients may respond better to a leukotriene receptor antagonist than to a long-acting β2-agonist. This is not readily predictable but such patients may include those with significant inflammation of the upper airways, as occurs with allergic rhinitis or nasal polyposis, 43 those with sensitivity to acetylsalicylic acid 44 and perhaps those with significant exercise-induced bronchoconstriction. 45 However, these responses are not consistent, and a trial of one medication, followed by a trial of the other if the first one fails, is a common approach.
Another option for add-on therapy is theophylline. This drug has been available for decades, but because of its narrow therapeutic window and frequent adverse effects, it is not commonly prescribed and should be reserved for patients in whom long-acting β2-agonist and leukotriene receptor antagonist therapy has failed. 4,8 The role of newer therapies such as anti-immunoglobulin E will be covered in a subsequent article in this series.
Outcome of the case
After satisfying yourself that Sara is using her inhaler properly, you decide to start her on an inhaler that combines an inhaled corticosteroid and a long-acting β2-agonist. There are 2 possible ways to use such therapy.
The first option, known as fixed therapy, has patients taking a set dose of medications on a regular basis and taking extra doses of fast-acting bronchodilators (e.g., salbutamol, formoterol) or higher doses of inhaled corticosteroid if their symptoms worsen. This can be accomplished with either of the combination inhalers available in Canada, fluticasone–salmeterol or budesonide–formoterol.
With the second option, a single inhaler is used for both maintenance and relief; only the budesonide–formoterol combination is suitable for this approach. In addition to the baseline maintenance dose of budesonide–formoterol, patients may use additional doses as a reliever medication over the course of the day to reduce the severity of acute symptoms and to reduce the frequency and severity of exacerbations. 46,47 This approach takes advantage of formoterol’s rapid onset, as well as the sustained activity and safety of the drug combination at higher doses. It is important to point out that this is not as-needed therapy for asthma, but rather as-needed addition of therapy to a stable maintenance dose of combination therapy.
Both fixed dosing and single-inhaler therapy for maintenance and relief of asthma lead to excellent outcomes for the patient if taken as prescribed. However, there is currently no way to predict which approach will work best in an individual patient. Compliance with prescribed therapy is likely to be higher if the patient is a partner in choosing which approach is taken and if appropriate use of the regimen is reinforced by a certified asthma educator.
Whenever the patient’s asthma therapy is changed, a follow-up visit within 1–3 months should be scheduled. At that follow-up visit, the clinician should assure compliance and proper inhalation technique, assess parameters of asthma control, review possible triggers for worsening of symptoms and review the components of the written action plan. In addition, once control of asthma has been achieved, the physician and patient may contemplate slowly reducing, but not stopping, maintenance therapy.
Gaps in knowledge and future directions
The key messages for the management of asthma in adults are presented in Box 3.
Clinical parameters and lung function alone cannot be used to determine which patients require higher doses of inhaled corticosteroids, either for maintenance therapy (as opposed to adding another class of medication) or for treatment of exacerbations. Distinguishing eosinophilic inflammation of the airways, which is typically found in asthma, from non-eosinophilic inflammation, which is typical of infectious and other conditions, may help physicians to better diagnose asthma and to treat exacerbations appropriately. Sputum cytology and determination of exhaled nitric oxide levels and possibly exhaled carbon monoxide levels are promising noninvasive tests that may help to guide therapy. 48–51 Use of these tests is currently limited to research institutions, and they are not funded for general use. Further research is required to prospectively define the role of these emerging tests in optimizing the diagnosis and management of asthma.
Several genes have been identified that predict susceptibility to asthma. These genes may operate by causing elevated production of immunoglobulin E, airway hyper-responsiveness or atopy through other mechanisms. 52–54 Other loci have been identified that may predict response to β2-agonists, 55 inhaled corticosteroids 56 and leukotriene antagonists. 57 The use of pharmacogenomics to predict which patients might respond best to a particular medication is the goal of current research but is probably years away from clinical utility.
There has been recent interest in the use of “as-needed” maintenance therapy for asthma. This involves patients not taking any anti-inflammatory agent on a regular basis but using an anti-inflammatory agent either alone or in combination with a bronchodilator when they have symptoms. Although some interesting and positive preliminary results have been obtained with this approach, 58,59 the studies so far have all been conducted in patients with mild persistent asthma. One study found similar improvement in peak flow with intermittent and daily use of inhaled corticosteroids in mild asthma, but superior suppression of inflammatory markers with regular use of inhaled corticosteroids. 58 Other important clinical end points, including exacerbations, were not examined. 58 The patient in this case, Sara, has more severe symptoms; as such, current evidence would not support considering her as a candidate for intermittent therapy.
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Low-dose inhaled corticosteroids are preferred as initial controller medication in the treatment of asthma.
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Leukotriene receptor antagonists should be prescribed for people with asthma who cannot or will not use inhaled corticosteroids.
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Long-acting β2-agonists should be prescribed only as a component of single-inhaler combination therapy for asthma (i.e., in combination with inhaled corticosteroid).
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For asthma not controlled with low-dose inhaled corticosteroids, combination therapy with long-acting β2-agonists and inhaled corticosteroids, in a single inhaler, is the preferred treatment choice.
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Patients with asthma should have regular follow-up visits, during which criteria for asthma control, compliance with medications and proper inhaler technique should be reviewed.
Key points
Articles to date in this series
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Subbarao P, Mandhane PJ, Sears MR. Asthma: epidemiology, etiology and risk factors. CMAJ 2009. www.cmaj.ca/cgi/doi/10.1503/cmaj.080612.
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Kaplan AG, Balter MS, Bell AD, et al. Diagnosis of asthma in adults. CMAJ 2009. www.cmaj.ca/cgi/doi/10.1503/cmaj.080006.
Footnotes
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Correspondence to: Dr. Meyer Balter, Mount Sinai Hospital, 600 University Ave., Suite 6-207, Toronto ON M5G 1X5; fax 416 586-4736; mbalter{at}mtsinai.on.ca
Previously published at www.cmaj.ca
This article has been peer reviewed.
Competing interests: Meyer Balter serves on advisory boards for AstraZeneca, Boehringer Ingelheim, GlaxoSmithKline, Merck Frosst, Nycomed and Pfizer and has received speaker fees from each of these companies over the past 2 years. Alan Bell has been a member of AstraZeneca Canada’s National Advisory Board for Respiratory Medicine from 2003 to the present and has received travel reimbursement to attend meetings of this board. He has also received consulting contracts and speaker fees from this board. He has received compensation for conducting clinical trials in respiratory disease from the following companies: AstraZeneca Canada, Nycomed Canada and Boehringer Ingelheim Canada. Alan Kaplan has received honoraria for talks from AstraZeneca, GlaxoSmithKline, Nycomed, Boehringer Ingelheim and Pfizer. He has served on advisory boards for Merck Frosst, Nycomed, AstraZeneca and Boehringer Ingelheim. He has received travel reimbursement to meetings of the European Respiratory Society from Merck and AstraZeneca. Harold Kim has received speaker fees and has served on advisory boards for Merck, GlaxoSmithKline, AstraZeneca, Graceway and Nycomed. Andrew McIvor has attended advisory board meetings and provided continuing medical education for which he has received honoraria from pharmaceutical companies involved in asthma management: AstraZeneca, Boehringer Ingelheim, Grace-way, GlaxoSmithKline, Novartis, Merck Frosst and Pfizer.
Contributors: All authors contributed to the development and editing of the publication, and all approved the version submitted for publication.
Funding: The Canadian Thoracic Society has received funding to facilitate the knowledge translation activities of the CTS Asthma Committee from AstraZeneca Canada, GlaxoSmithKline Inc., Merck Frosst Canada and Novartis Pharmaceuticals. None of the sponsors played a role in the collection, review, analysis or interpretation of the scientific literature or in any decisions regarding the key messages presented in the case studies.
This article is the third in a 7-part case study series that was developed as a knowledge translation initiative of the Canadian Thoracic Society Asthma Committee. The series aims to educate and inform primary care providers and nonrespiratory specialists about the diagnosis and management of asthma. The key messages presented in the cases are not clinical practice guidelines but are based on a review of the most recent scientific evidence available. Financial support for the publication of this series has been provided, in part, by the Canadian Thoracic Society.